Rearrangements of the Benzilic Acid Type; Preparation and Use of Dialkali Metal Adducts of Aromatic Ketones.
Date Issued
August 1, 1959
Author(s)
Selman, Stanley
Advisor(s)
Jerome F. Eastham
Additional Advisor(s)
D. A. Shirley
Carl Buehler
John W. Prados
Abstract
Introduction: The benzilic acid rearrangement is the base-catalyzed transformation of an α-diketone to the salt of an α-hydroxy acid. This rearrangement can be effected in aromatic, semi-aromatic (o-quinones), in alicyclic, and aliphatic, as well as in heterocyclic α-diketones. Examples of the rearrangement in the above type compounds are illustrated in equations 1-6.
Disciplines
Degree
Doctor of Philosophy
Major
Chemistry
Embargo Date
August 1, 1959
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SelmanStanley_1959_OCRed.pdf
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